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Phrenilin Forte
Phrenilin Forte - 0187-0844-02 - (Butalbital and Acetaminophen)
Drug Information of Phrenilin Forte
| Product NDC: | 0187-0844 |
| Proprietary Name: | Phrenilin Forte |
| Non Proprietary Name: | Butalbital and Acetaminophen |
| Active Ingredient(s): | 650; 50 mg/1; mg/1 & nbsp; Butalbital and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phrenilin Forte
| Product NDC: | 0187-0844 |
| Labeler Name: | Valeant Pharmaceuticals International |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088831 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040503 |
Package Information of Phrenilin Forte
| Package NDC: | 0187-0844-02 |
| Package Description: | 500 CAPSULE in 1 BOTTLE, PLASTIC (0187-0844-02) |
NDC Information of Phrenilin Forte
| NDC Code | 0187-0844-02 |
| Proprietary Name | Phrenilin Forte |
| Package Description | 500 CAPSULE in 1 BOTTLE, PLASTIC (0187-0844-02) |
| Product NDC | 0187-0844 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Butalbital and Acetaminophen |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20040503 |
| Marketing Category Name | ANDA |
| Labeler Name | Valeant Pharmaceuticals International |
| Substance Name | ACETAMINOPHEN; BUTALBITAL |
| Strength Number | 650; 50 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Barbiturate [EPC],Barbiturates [Chemical/Ingredient] |
